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Moderna

Develops mRNA-based medicines for health

Quality Assurance & Compliance Co-op

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Internship · Winter 2027, Spring 2027Norwood, MA, USA

About the Job

Requirements

  • The candidate must be a current student enrolled in a Bachelor's or Master's program in a science-related field or Regulatory Affairs.
  • The candidate should have an interest in learning about cGMP manufacturing, quality systems, batch record review, deviation management, and inspection management.
  • The candidate must have strong written and verbal communication skills, attention to detail, a collaborative mindset, and willingness to ask questions and escalate quality or safety concerns appropriately.
  • The candidate must be available for the entire co-op duration.
  • The candidate must already hold U.S. work authorization and be able to maintain that status without future sponsorship.
  • The candidate must qualify as a U.S. person under export control rules (citizen, permanent resident, asylee, or refugee) to access export-controlled information.

Responsibilities

  • Support compliance activities and learn the fundamentals of quality systems.
  • Collaborate with Quality and cross-functional teams on daily activities and improvement projects.
  • Help draft and review SOPs, policies, batch records, testing records, and training materials.
  • Review electronic and paper batch records for completeness and cGMP compliance.
  • Observe manufacturing activities and support compliance with procedures, specifications, and cleanroom practices.
  • Follow written procedures and maintain clear, accurate, and complete documentation.
  • Complete required training and follow data integrity principles.
  • Identify and promptly escalate manufacturing, safety, and quality concerns.
  • Support deviation documentation, investigations, and corrective actions.
  • Support regulatory and inspection readiness activities, including internal audits and health authority engagement.
  • Collect, analyze, and report quality metrics to identify trends and improvement opportunities.
  • Use problem-solving skills to support quality and operational improvements.
  • Lead assigned quality projects from planning through completion with guidance.
  • Manage priorities and contribute to multiple projects at the same time.
  • Follow Moderna's safety procedures and practice safe work habits.
  • Perform additional duties as assigned.

Desired Qualifications

  • A GPA of 3.5 on a 4.0 scale or equivalent is preferred.
  • The candidate should be able to work independently and contribute to high-performing teams.

About the Company

Moderna

Develops mRNA-based medicines for health

Moderna develops medicines built on messenger RNA (mRNA). Its products use mRNA delivered into cells to instruct them to produce specific proteins that can prevent or treat disease, with vaccines being a primary example. In practice, a dose delivers engineered mRNA into the body, cells translate it into a target protein, and the immune system responds or the protein modulates biology to combat disease. Moderna differentiates itself through its focus on building a whole mRNA medicines platform and in-house capabilities for designing, manufacturing, and scaling mRNA therapies, including rapid development and large-scale production. Its goal is to create a new category of medicines based on mRNA that can improve how diseases are discovered, developed, and treated, ultimately improving patient outcomes.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2010

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